FDA 510(k)

SPLIT TOP WING NEEDLE CAP WITH OPTIONAL TUBING ANCHORS (AND APPROPRIATE RECAP DEVICE

K-Number: K944680 · 1995-01-31

ApplicantResearched, Novel Medical Devices (Rn/Md)

Decision Date1995-01-31

Product CodeFMI

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

SPLIT TOP WING NEEDLE CAP WITH OPTIONAL TUBING ANCHORS (AND APPROPRIATE RECAP DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Researched, Novel Medical Devices (Rn/Md). It received FDA 510(k) clearance on 1995-01-31 under 510(k) number K944680. The device is classified under product code FMI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SPLIT TOP WING NEEDLE CAP WITH OPTIONAL TUBING ANCHORS (AND APPROPRIATE RECAP DEVICE?

SPLIT TOP WING NEEDLE CAP WITH OPTIONAL TUBING ANCHORS (AND APPROPRIATE RECAP DEVICE is a medical device that received FDA 510(k) clearance on 1995-01-31. The listed applicant is Researched, Novel Medical Devices (Rn/Md). The 510(k) number is K944680.

When did SPLIT TOP WING NEEDLE CAP WITH OPTIONAL TUBING ANCHORS (AND APPROPRIATE RECAP DEVICE receive FDA 510(k) clearance?

SPLIT TOP WING NEEDLE CAP WITH OPTIONAL TUBING ANCHORS (AND APPROPRIATE RECAP DEVICE received FDA 510(k) clearance on 1995-01-31, under 510(k) number K944680.

Who is the listed applicant for SPLIT TOP WING NEEDLE CAP WITH OPTIONAL TUBING ANCHORS (AND APPROPRIATE RECAP DEVICE?

The FDA 510(k) record lists Researched, Novel Medical Devices (Rn/Md) as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SPLIT TOP WING NEEDLE CAP WITH OPTIONAL TUBING ANCHORS (AND APPROPRIATE RECAP DEVICE?

The FDA product code for SPLIT TOP WING NEEDLE CAP WITH OPTIONAL TUBING ANCHORS (AND APPROPRIATE RECAP DEVICE is FMI.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.